KR20010101661A - 메틸 카르바제이트의 제조 방법 - Google Patents
메틸 카르바제이트의 제조 방법 Download PDFInfo
- Publication number
- KR20010101661A KR20010101661A KR1020017009303A KR20017009303A KR20010101661A KR 20010101661 A KR20010101661 A KR 20010101661A KR 1020017009303 A KR1020017009303 A KR 1020017009303A KR 20017009303 A KR20017009303 A KR 20017009303A KR 20010101661 A KR20010101661 A KR 20010101661A
- Authority
- KR
- South Korea
- Prior art keywords
- hydrazine
- solvent
- dimethyl carbonate
- methyl carbazate
- process according
- Prior art date
Links
- WFJRIDQGVSJLLH-UHFFFAOYSA-N methyl n-aminocarbamate Chemical compound COC(=O)NN WFJRIDQGVSJLLH-UHFFFAOYSA-N 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims description 28
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims abstract description 56
- 239000002904 solvent Substances 0.000 claims abstract description 27
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 238000004821 distillation Methods 0.000 claims abstract description 12
- 239000000376 reactant Substances 0.000 claims abstract description 9
- 238000009835 boiling Methods 0.000 claims abstract description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 150000007824 aliphatic compounds Chemical class 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- 150000001491 aromatic compounds Chemical class 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 239000003570 air Substances 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims 1
- 238000002845 discoloration Methods 0.000 abstract description 4
- 239000011261 inert gas Substances 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000000203 mixture Substances 0.000 description 7
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 4
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000010977 jade Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- -1 methyl carbon Chemical compound 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/02—Compounds containing any of the groups, e.g. carbazates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19902960A DE19902960A1 (de) | 1999-01-26 | 1999-01-26 | Verfahren zur Herstellung von Methylcarbazat |
| DE19902960.1 | 1999-01-26 | ||
| PCT/EP2000/000310 WO2000044708A1 (de) | 1999-01-26 | 2000-01-17 | Verfahren zur herstellung von methylcarbazat |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20010101661A true KR20010101661A (ko) | 2001-11-14 |
Family
ID=7895390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020017009303A KR20010101661A (ko) | 1999-01-26 | 2000-01-17 | 메틸 카르바제이트의 제조 방법 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US6465678B1 (de) |
| EP (1) | EP1149070B1 (de) |
| JP (1) | JP4399119B2 (de) |
| KR (1) | KR20010101661A (de) |
| CN (1) | CN1337943A (de) |
| AT (1) | ATE243678T1 (de) |
| AU (1) | AU749982B2 (de) |
| BR (1) | BR0007682A (de) |
| CA (1) | CA2361423A1 (de) |
| DE (2) | DE19902960A1 (de) |
| DK (1) | DK1149070T3 (de) |
| ES (1) | ES2197072T3 (de) |
| HU (1) | HUP0105200A3 (de) |
| IL (1) | IL143872A0 (de) |
| PL (1) | PL348889A1 (de) |
| WO (1) | WO2000044708A1 (de) |
| ZA (1) | ZA200105035B (de) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100341598C (zh) * | 2004-12-22 | 2007-10-10 | 上海氯碱化工股份有限公司 | 一种低温蒸发、冷却生产超净高纯试剂的方法 |
| CN100408554C (zh) * | 2005-11-01 | 2008-08-06 | 北京格瑞华阳科技发展有限公司 | 高纯度肼基碳酸甲酯的合成新工艺 |
| CN101260067B (zh) * | 2007-03-07 | 2010-09-01 | 抚顺市化工研究设计院 | 一种肼单甲基化的方法 |
| CN101628184B (zh) * | 2009-03-18 | 2013-08-14 | 伍运洪 | 一种常压低温蒸馏、精馏工艺 |
| WO2011005910A1 (en) * | 2009-07-09 | 2011-01-13 | The Procter & Gamble Company | Method of laundering fabric using a compacted laundry detergent composition |
| CN102153490A (zh) * | 2011-02-16 | 2011-08-17 | 东营柯林维尔化工有限公司 | 肼基甲酸酯类的合成 |
| JP5790533B2 (ja) * | 2012-02-14 | 2015-10-07 | 住友化学株式会社 | フェニルヒドラジン−β−カルボキシレート化合物の精製方法 |
| CN102898328B (zh) * | 2012-10-26 | 2014-12-24 | 山东师范大学 | 偶氮二甲酸二乙酯及其中间体的合成方法 |
| CN103130687A (zh) * | 2013-03-19 | 2013-06-05 | 湖南斯派克材料科技有限公司 | 肼甲酸甲酯的制备方法 |
| CN103819366B (zh) * | 2014-02-19 | 2016-08-24 | 江苏辉腾生物医药科技有限公司 | 肼基甲酸苄酯的合成方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE285800C (de) | ||||
| SU407888A1 (ru) | 1972-02-16 | 1973-12-10 | Способ получения гя?г-бутилового эфира гидразинугольной кислоты | |
| US4496761A (en) | 1982-08-17 | 1985-01-29 | Olin Corporation | Process for making carbohydrazide |
| YU44721B (en) | 1983-11-30 | 1990-12-31 | Bristol Myers Co | Process for obtaining 4-(2-phenoxyethyl)-1,2,4-triazolone |
| US4596884A (en) * | 1983-11-30 | 1986-06-24 | Bristol-Myers Company | 4-(2-phenoxyethyl)-1,2,4-triazolone process intermediates |
-
1999
- 1999-01-26 DE DE19902960A patent/DE19902960A1/de not_active Withdrawn
-
2000
- 2000-01-17 KR KR1020017009303A patent/KR20010101661A/ko not_active Application Discontinuation
- 2000-01-17 AU AU25419/00A patent/AU749982B2/en not_active Ceased
- 2000-01-17 IL IL14387200A patent/IL143872A0/xx unknown
- 2000-01-17 DK DK00903582T patent/DK1149070T3/da active
- 2000-01-17 BR BR0007682-1A patent/BR0007682A/pt not_active IP Right Cessation
- 2000-01-17 HU HU0105200A patent/HUP0105200A3/hu unknown
- 2000-01-17 WO PCT/EP2000/000310 patent/WO2000044708A1/de not_active Application Discontinuation
- 2000-01-17 DE DE50002642T patent/DE50002642D1/de not_active Expired - Lifetime
- 2000-01-17 CN CN00803141A patent/CN1337943A/zh active Pending
- 2000-01-17 ES ES00903582T patent/ES2197072T3/es not_active Expired - Lifetime
- 2000-01-17 JP JP2000595965A patent/JP4399119B2/ja not_active Expired - Fee Related
- 2000-01-17 EP EP00903582A patent/EP1149070B1/de not_active Expired - Lifetime
- 2000-01-17 PL PL00348889A patent/PL348889A1/xx unknown
- 2000-01-17 CA CA002361423A patent/CA2361423A1/en not_active Abandoned
- 2000-01-17 AT AT00903582T patent/ATE243678T1/de not_active IP Right Cessation
- 2000-01-17 US US09/889,813 patent/US6465678B1/en not_active Expired - Lifetime
-
2001
- 2001-06-20 ZA ZA200105035A patent/ZA200105035B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE243678T1 (de) | 2003-07-15 |
| AU749982B2 (en) | 2002-07-04 |
| WO2000044708A1 (de) | 2000-08-03 |
| DK1149070T3 (da) | 2003-09-29 |
| EP1149070A1 (de) | 2001-10-31 |
| US6465678B1 (en) | 2002-10-15 |
| AU2541900A (en) | 2000-08-18 |
| JP2002535381A (ja) | 2002-10-22 |
| JP4399119B2 (ja) | 2010-01-13 |
| DE19902960A1 (de) | 2000-07-27 |
| CA2361423A1 (en) | 2000-08-03 |
| ZA200105035B (en) | 2002-06-20 |
| DE50002642D1 (de) | 2003-07-31 |
| BR0007682A (pt) | 2001-11-06 |
| IL143872A0 (en) | 2002-04-21 |
| PL348889A1 (en) | 2002-06-17 |
| EP1149070B1 (de) | 2003-06-25 |
| HUP0105200A2 (hu) | 2002-04-29 |
| HUP0105200A3 (en) | 2002-12-28 |
| ES2197072T3 (es) | 2004-01-01 |
| CN1337943A (zh) | 2002-02-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |